A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616995



Internal ID18568590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196371892..196687288hg38UCSC Ensembl
Innerchr3:196098763..196414159hg19UCSC Ensembl
Innerchr3:197583160..197898556hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38315397
hg19315397
hg18315397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003066
Supporting Variants
Samples
Known GenesC3orf43, FBXO45, NRROS, RNF168, UBXN7, WDR53
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616995
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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